rs154774640
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs154774640(C;G) |
Make rs154774640(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 68218584 |
Gene | CLN6 |
is a | snp |
is | mentioned by |
dbSNP | rs154774640 |
dbSNP (classic) | rs154774640 |
ClinGen | rs154774640 |
ebi | rs154774640 |
HLI | rs154774640 |
Exac | rs154774640 |
Gnomad | rs154774640 |
Varsome | rs154774640 |
LitVar | rs154774640 |
Map | rs154774640 |
PheGenI | rs154774640 |
Biobank | rs154774640 |
1000 genomes | rs154774640 |
hgdp | rs154774640 |
ensembl | rs154774640 |
geneview | rs154774640 |
scholar | rs154774640 |
rs154774640 | |
pharmgkb | rs154774640 |
gwascentral | rs154774640 |
openSNP | rs154774640 |
23andMe | rs154774640 |
SNPshot | rs154774640 |
SNPdbe | rs154774640 |
MSV3d | rs154774640 |
GWAS Ctlg | rs154774640 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs154774640(G;G) |
Alt | rs154774640(G;G) |
Reference | Rs154774640(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CLN6 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000015.9:g.68510922G>C |
CLNSRC | |
CLNACC | RCV000058908.1, |